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Literature DB >> 11674384

Syntheses of D- and L-Mannose, Gulose, and Talose via Diastereoselective and Enantioselective Dihydroxylation Reactions.

Joel M. Harris¹, Mark D. Keranen, George A. O'Doherty.

Abstract

Entities: Chemical

Year: 1999 PMID： 11674384 DOI： 10.1021/jo990410+

Source DB: PubMed Journal: J Org Chem ISSN： 0022-3263 Impact factor: 4.354

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16 in total

1. De novo asymmetric synthesis of the mezzettiaside family of natural products via the iterative use of a dual B-/Pd-catalyzed glycosylation.

Authors: Sumit O Bajaj; Ehesan U Sharif; Novruz G Akhmedov; George A O'Doherty
Journal: Chem Sci Date: 2014-06 Impact factor: 9.825

2. Synthesis of several cleistrioside and cleistetroside natural products via a divergent de novo asymmetric approach.

Authors: Bulan Wu; Miaosheng Li; George A O'Doherty
Journal: Org Lett Date: 2010-11-01 Impact factor: 6.005

3. De novo asymmetric syntheses of D- and L-talose via an iterative dihydroxylation of dienoates.

Authors: Md Moinuddin Ahmed; George A O'Doherty
Journal: J Org Chem Date: 2005-12-09 Impact factor: 4.354

4. Synthesis and Structure-Activity Relationship Study of 5a-Carbasugar Analogues of SL0101.

Authors: Mingzong Li; Yu Li; Roman M Mrozowski; Zachary M Sandusky; Mingde Shan; Xiwen Song; Bulan Wu; Qi Zhang; Deborah A Lannigan; George A O'Doherty
Journal: ACS Med Chem Lett Date: 2014-11-26 Impact factor: 4.345

5. De novo asymmetric syntheses of SL0101 and its analogues via a palladium-catalyzed glycosylation.

Authors: Mingde Shan; George A O'Doherty
Journal: Org Lett Date: 2006-10-26 Impact factor: 6.005

6. Developing a diastereoselective intramolecular [4+3] cycloaddition of nitrogen-stabilized oxyallyl cations derived from N-sulfonyl-substituted allenamides.

Authors: Andrew G Lohse; Richard P Hsung; Mitchell D Leider; Sunil K Ghosh
Journal: J Org Chem Date: 2011-04-08 Impact factor: 4.354

Syntheses of D- and L-Mannose, Gulose, and Talose via Diastereoselective and Enantioselective Dihydroxylation Reactions.

1. De novo asymmetric synthesis of the mezzettiaside family of natural products via the iterative use of a dual B-/Pd-catalyzed glycosylation.

2. Synthesis of several cleistrioside and cleistetroside natural products via a divergent de novo asymmetric approach.

3. De novo asymmetric syntheses of D- and L-talose via an iterative dihydroxylation of dienoates.

4. Synthesis and Structure-Activity Relationship Study of 5a-Carbasugar Analogues of SL0101.

5. De novo asymmetric syntheses of SL0101 and its analogues via a palladium-catalyzed glycosylation.

6. Developing a diastereoselective intramolecular [4+3] cycloaddition of nitrogen-stabilized oxyallyl cations derived from N-sulfonyl-substituted allenamides.

7. Achmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.

Review 8. De novo synthesis of natural products via the asymmetric hydration of polyenes.

9. De novo asymmetric synthesis of all-D-, all-L-, and D-/L-oligosaccharides using atom-less protecting groups.

Review 10. Synthesis and biological study of the phomopsolide and phomopsolidone natural products.